REGULATION 2020 revision
Provisions for Drug Registration
ABSTRACT — EDITORS' SUMMARY
The umbrella drug registration regulation in English. Article 107 mandates routine GCP inspections of clinical trial organisations. GCP-relevant sections cover sponsor obligations, ethics review, and clinical trial conduct.
EXTERNAL LINK
EXTERNAL LINK english.nmpa.gov.cn
↗ METADATA
SOURCE
LINK · CANONICAL LINK https://english.nmpa.gov.cn/2022-06/30/c_785628_8.htm ↗ RELATED · SAME AUTHORITY